These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

452 related articles for article (PubMed ID: 6326308)

  • 1. [The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis].
    Adrien A; Guillet G
    Sem Hop; 1984 Apr; 60(16):1148-52. PubMed ID: 6326308
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Porphyria cutanea tarda].
    Perrot H
    Ann Dermatol Venereol; 1987; 114(8):1023-6. PubMed ID: 3426071
    [No Abstract]   [Full Text] [Related]  

  • 3. The enzymatic defects in porphyria cutanea tarda and variegate porphyria.
    Kushner JP
    Acta Derm Venereol Suppl (Stockh); 1982; 100():51-6. PubMed ID: 6962633
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda.
    Felsher BF; Carpio NM; Engleking DW; Nunn AT
    N Engl J Med; 1982 Apr; 306(13):766-9. PubMed ID: 7062951
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family.
    Lazaro P; de Salamanca RE; Elder GH; Villaseca ML; Chinarro S; Jaqueti G
    Br J Dermatol; 1984 May; 110(5):613-7. PubMed ID: 6722030
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria.
    de Verneuil H; Beaumont C; Deybach JC; Nordmann Y; Sfar Z; Kastally R
    Am J Hum Genet; 1984 May; 36(3):613-22. PubMed ID: 6375356
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects.
    Elder GH; Roberts AG; de Salamanca RE
    Clin Biochem; 1989 Jun; 22(3):163-8. PubMed ID: 2786774
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chronic hepatic porphyria with uroporphyrinogen decarboxylase defect in four generations (author's transl)].
    Lehr PA; Doss M
    Dtsch Med Wochenschr; 1981 Feb; 106(8):241-5. PubMed ID: 7472211
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Early forms of porphyria cutanea tarda. Apropos of 2 cases with a study of familial enzymatic deficiency and definition of the mode of genetic transmission].
    Herrero C; Muniesa AM; Lecha M; Elder GH; Mascaro JM
    Ann Dermatol Venereol; 1984; 111(11):973-8. PubMed ID: 6524816
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The enzymatic defect in porphyria cutanea tarda.
    Kushner JP
    N Engl J Med; 1982 Apr; 306(13):799-800. PubMed ID: 7062954
    [No Abstract]   [Full Text] [Related]  

  • 11. An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.
    Kushner JP; Barbuto AJ; Lee GR
    J Clin Invest; 1976 Nov; 58(5):1089-97. PubMed ID: 993332
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria.
    de Verneuil H; Grandchamp B; Romeo PH; Raich N; Beaumont C; Goossens M; Nicolas H; Nordmann Y
    J Clin Invest; 1986 Feb; 77(2):431-5. PubMed ID: 3753711
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Porphyria cutanea tarda in a 4-year-old child with uroporphyrinogen decarboxylase deficiency].
    Cotton JB; Abeille A; Jeune R; Ladreyt-Ponchon JP; Grenier JL
    Pediatrie; 1986 Dec; 41(8):617-27. PubMed ID: 3575073
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hereditary porphyria cutanea in children. Enzymatic studies (author's transl)].
    Doutre MS; Beylot C; Bioulac P; Nordmann Y
    Ann Dermatol Venereol; 1981; 108(10):751-7. PubMed ID: 7305216
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
    Elder GH; Lee GB; Tovey JA
    N Engl J Med; 1978 Aug; 299(6):274-8. PubMed ID: 661926
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Porphyria cutanea tarda (PCT)].
    Goerz G; Merk H
    Z Hautkr; 1985 Jan; 60(1-2):137-46. PubMed ID: 3885597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Steady-state levels of uroporphyrinogen decarboxylase mRNA in lymphoblastoid cell lines from patients with familial porphyria cutanea tarda and their relatives.
    Hansen JL; Pryor MA; Kennedy JB; Kushner JP
    Am J Hum Genet; 1988 Jun; 42(6):847-53. PubMed ID: 3369447
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Uroporphyrinogen decarboxylase deficiency in hepatoerythropoietic porphyria: further evidence for genetic heterogeneity.
    Kószó F; Elder GH; Roberts A; Simon N
    Br J Dermatol; 1990 Mar; 122(3):365-70. PubMed ID: 2322500
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dual porphyria in double heterozygotes with porphobilinogen deaminase and uroporphyrinogen decarboxylase deficiencies.
    Doss MO
    Clin Genet; 1989 Feb; 35(2):146-51. PubMed ID: 2721023
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Porphyria cutanea tarda: erythrocyte uroporphyrinogen decarboxylase activity in 471 consecutive patients.
    Doss MO; Frank M; Braun-Falco O
    Curr Probl Dermatol; 1991; 20():97-105. PubMed ID: 1935224
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 23.